JP7089516B2 - ある特定のレベルのバイオベース炭素を含むポリマー - Google Patents
ある特定のレベルのバイオベース炭素を含むポリマー Download PDFInfo
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- JP7089516B2 JP7089516B2 JP2019530752A JP2019530752A JP7089516B2 JP 7089516 B2 JP7089516 B2 JP 7089516B2 JP 2019530752 A JP2019530752 A JP 2019530752A JP 2019530752 A JP2019530752 A JP 2019530752A JP 7089516 B2 JP7089516 B2 JP 7089516B2
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- 229920000642 polymer Polymers 0.000 title claims description 187
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims description 109
- 229910052799 carbon Inorganic materials 0.000 title claims description 104
- 239000000178 monomer Substances 0.000 claims description 127
- 125000004432 carbon atom Chemical group C* 0.000 claims description 105
- 239000000203 mixture Substances 0.000 claims description 96
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 50
- -1 or Q + is Li + Substances 0.000 claims description 49
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 claims description 40
- 238000010348 incorporation Methods 0.000 claims description 38
- 230000007935 neutral effect Effects 0.000 claims description 33
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 32
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 29
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 24
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 23
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- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 claims description 21
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- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 11
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 claims description 10
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 9
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- 238000006386 neutralization reaction Methods 0.000 claims description 9
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- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
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- 239000004034 viscosity adjusting agent Substances 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
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- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 26
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- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 19
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 18
- 235000011187 glycerol Nutrition 0.000 description 18
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- 239000002904 solvent Substances 0.000 description 17
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- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 13
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- UXRNWUYCCQFHIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C UXRNWUYCCQFHIH-UHFFFAOYSA-N 0.000 description 12
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- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
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- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
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- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
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- 229940105990 diglycerin Drugs 0.000 description 1
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- RXNWFGQCYAZACC-UHFFFAOYSA-L dilithium;2-methylidenebutanedioate Chemical compound [Li+].[Li+].[O-]C(=O)CC(=C)C([O-])=O RXNWFGQCYAZACC-UHFFFAOYSA-L 0.000 description 1
- RBYDCVNTVVKIQT-UHFFFAOYSA-L dipotassium;2-methylidenebutanedioate Chemical compound [K+].[K+].[O-]C(=O)CC(=C)C([O-])=O RBYDCVNTVVKIQT-UHFFFAOYSA-L 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
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- 239000003456 ion exchange resin Substances 0.000 description 1
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- 150000002576 ketones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 229910000032 lithium hydrogen carbonate Inorganic materials 0.000 description 1
- HQRPHMAXFVUBJX-UHFFFAOYSA-M lithium;hydrogen carbonate Chemical compound [Li+].OC([O-])=O HQRPHMAXFVUBJX-UHFFFAOYSA-M 0.000 description 1
- KMGUUVHVXYFYQN-UHFFFAOYSA-L magnesium;2-methylidenebutanedioate Chemical compound [Mg+2].[O-]C(=O)CC(=C)C([O-])=O KMGUUVHVXYFYQN-UHFFFAOYSA-L 0.000 description 1
- DWLAVVBOGOXHNH-UHFFFAOYSA-L magnesium;prop-2-enoate Chemical compound [Mg+2].[O-]C(=O)C=C.[O-]C(=O)C=C DWLAVVBOGOXHNH-UHFFFAOYSA-L 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- FYGDTMLNYKFZSV-UHFFFAOYSA-N mannotriose Natural products OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(OC2C(OC(O)C(O)C2O)CO)C(O)C1O FYGDTMLNYKFZSV-UHFFFAOYSA-N 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000001471 micro-filtration Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- BSCJIBOZTKGXQP-UHFFFAOYSA-N n-(2-hydroxyethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCO BSCJIBOZTKGXQP-UHFFFAOYSA-N 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 description 1
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
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- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- AMLFJZRZIOZGPW-UHFFFAOYSA-N prop-1-en-1-amine Chemical compound CC=CN AMLFJZRZIOZGPW-UHFFFAOYSA-N 0.000 description 1
- CXNQUHPJUJGOHC-UHFFFAOYSA-J prop-2-enoate;zirconium(4+) Chemical compound [Zr+4].[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C.[O-]C(=O)C=C CXNQUHPJUJGOHC-UHFFFAOYSA-J 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 235000011962 puddings Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
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- 210000003491 skin Anatomy 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
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- 238000012360 testing method Methods 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 238000000108 ultra-filtration Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
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- 238000005406 washing Methods 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/58—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine
- C08F220/585—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing oxygen in addition to the carbonamido oxygen, e.g. N-methylolacrylamide, N-(meth)acryloylmorpholine and containing other heteroatoms, e.g. 2-acrylamido-2-methylpropane sulfonic acid [AMPS]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8164—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers, e.g. poly (methyl vinyl ether-co-maleic anhydride)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/10—Copolymer characterised by the proportions of the comonomers expressed as molar percentages
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Dermatology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16203555.4 | 2016-12-12 | ||
| EP16203555 | 2016-12-12 | ||
| PCT/EP2017/081414 WO2018108608A1 (fr) | 2016-12-12 | 2017-12-04 | Polymère comprenant une certaine quantité de carbone biosourcé |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2020513461A JP2020513461A (ja) | 2020-05-14 |
| JP7089516B2 true JP7089516B2 (ja) | 2022-06-22 |
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| JP2019530752A Active JP7089516B2 (ja) | 2016-12-12 | 2017-12-04 | ある特定のレベルのバイオベース炭素を含むポリマー |
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| Country | Link |
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| US (1) | US20200009041A1 (fr) |
| EP (1) | EP3551679B1 (fr) |
| JP (1) | JP7089516B2 (fr) |
| CN (1) | CN110267997B (fr) |
| WO (1) | WO2018108608A1 (fr) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112017024689B1 (pt) | 2015-06-17 | 2022-04-12 | Clariant International Ltd | Polímeros hidrossolúveis ou incháveis em água, seu processo de produção, seu uso, processo de cimentação de perfurações profundas utilizando uma lama de cimento e mistura polimérica |
| CN109563030B (zh) | 2016-06-20 | 2022-06-10 | 科莱恩国际有限公司 | 包含一定水平的生物基碳的化合物 |
| JP7032402B2 (ja) | 2016-12-12 | 2022-03-08 | クラリアント・インターナシヨナル・リミテツド | ある特定のレベルのバイオベース炭素を含むポリマー |
| EP3551163B1 (fr) * | 2016-12-12 | 2021-02-17 | Clariant International Ltd | Utilisation d'un polymère d'origine biologique dans une composition cosmétique, dermatologique ou pharmaceutique |
| US11542343B2 (en) | 2016-12-15 | 2023-01-03 | Clariant International Ltd | Water-soluble and/or water-swellable hybrid polymer |
| WO2018108667A1 (fr) | 2016-12-15 | 2018-06-21 | Clariant International Ltd | Polymère hybride hydrosoluble et/ou gonflable dans l'eau |
| EP3554643A1 (fr) | 2016-12-15 | 2019-10-23 | Clariant International Ltd | Polymère hybride hydrosoluble et/ou gonflable dans l'eau |
| US11401362B2 (en) | 2016-12-15 | 2022-08-02 | Clariant International Ltd | Water-soluble and/or water-swellable hybrid polymer |
| FR3113907B1 (fr) * | 2020-09-07 | 2023-05-05 | Snf Sa | Utilisation dans des compositions hydroalcooliques d’un copolymere obtenu par polymerisation par precipitation |
| EP4367197A1 (fr) * | 2021-07-09 | 2024-05-15 | SNF Group | Polymere d'acide 2-acrylamido-2-methylpropane sulfonique et leur utilisation |
| FR3125041A1 (fr) | 2021-07-09 | 2023-01-13 | Snf Sa | Procédé d’obtention de N-vinylformamide biosourcé |
| CN115819734A (zh) * | 2022-10-26 | 2023-03-21 | 西湖大学 | 一类含两性离子侧链结构的阴离子交换聚合物及其应用 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009149536A (ja) | 2007-12-19 | 2009-07-09 | Toagosei Co Ltd | ２−アクリルアミド−２−メチルプロパンスルホン酸の連続製造方法 |
| JP2012521448A (ja) | 2009-03-25 | 2012-09-13 | クラリアント・ファイナンス・（ビーブイアイ）・リミテッド | アクリル−、メタクリル−もしくはエタクリルアミドアルキルスルホン酸、またはその塩、およびカルボキシアルキルアクリラート、−メタクリラートまたは−エタクリラート、あるいはこれらカルボキシ化合物のオリゴマーに基づくポリマー |
| JP2014511423A (ja) | 2011-03-08 | 2014-05-15 | クラリアント・ファイナンス・（ビーブイアイ）・リミテッド | スルホン酸、アミド及び特定の架橋剤をベースとするポリマー |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA718025A (en) | 1959-02-24 | 1965-09-14 | The Standard Oil Company | Process for the manufacture of acrylonitrile |
| CA1076144A (fr) | 1975-12-09 | 1980-04-22 | Alvin B. Stiles | Procede pour l'oxydation du 1-propanol |
| EP0750899A3 (fr) * | 1995-06-30 | 1998-05-20 | Shiseido Company Limited | Agent émulsionnant ou agent solubilisant qui est composé du polyélectrolyte amphiphile soluble dans l'eau et composition émulsifié le contenant ou composition solubilisé le contenant et cosmétique émulsifié le contenant ou cosmétique solubilisé le contenant |
| FR2750325B1 (fr) | 1996-06-28 | 1998-07-31 | Oreal | Utilisation en cosmetique d'un poly(acide 2-acrylamido 2- methylpropane sulfonique) reticule et neutralise a au moins 90 % et compositions topiques les contenant |
| DE19625810A1 (de) | 1996-06-28 | 1998-01-02 | Hoechst Ag | Wasserlösliche oder wasserquellbare Polymerisate |
| DE10322269A1 (de) * | 2003-05-16 | 2004-12-02 | Clariant Gmbh | Flüssige Wasch- und Reinigungsmittel mit Konsistenzgebenden Polymeren |
| DE102004035515A1 (de) * | 2004-07-22 | 2006-02-16 | Clariant Gmbh | Thermostabiles, wasserlösliches, bei hohen Temperaturen vernetzbares Polymer |
| FR2912742B1 (fr) | 2007-02-16 | 2010-03-05 | Arkema France | Procede de synthese d'acrylonitrile a partir de glycerol |
| ES2319949B1 (es) | 2007-11-13 | 2010-03-17 | Consejo Superior De Investigaciones Cientificas | Proceso catalitico de produccion de nitrilos a partir de alcoholes. |
| WO2009072480A1 (fr) * | 2007-12-06 | 2009-06-11 | Toagosei Co., Ltd. | Acide 2-acrylamide-2-méthylpropanesulfonique et son procédé de fabrication |
| DE102007061969A1 (de) * | 2007-12-21 | 2008-07-17 | Clariant International Limited | Wasserlösliche oder wasserquellbare Polymere auf Basis von Salzen der Acryloyldimethyltaurinsäure oder ihrer Derivate, deren Herstellung und deren Verwendung als Verdicker, Stabilisator und Konsistenzgeber |
| FR2931822B1 (fr) | 2008-05-30 | 2012-11-02 | Arkema France | Methacrylate de methyle derive de la biomasse, procede de fabrication, utilisations et polymeres correspondants. |
| DE102008034102A1 (de) * | 2008-07-21 | 2010-01-28 | Henkel Ag & Co. Kgaa | Geschmeidiges Stylingmittel mit hohem Haltegrad |
| TW201229060A (en) * | 2010-10-01 | 2012-07-16 | Lanxess Deutschland Gmbh | Polymers of isobutene from renewable sources |
| WO2012084977A1 (fr) * | 2010-12-20 | 2012-06-28 | Dsm Ip Assets B.V. | Billes vinyliques bio-renouvelables |
| JP2015507048A (ja) * | 2012-02-03 | 2015-03-05 | ディーエスエム アイピー アセッツ ビー．ブイ． | ポリマー組成物の使用 |
| WO2014004616A2 (fr) | 2012-06-26 | 2014-01-03 | Gevo, Inc. | Levure génétiquement modifiée ayant une croissance améliorée dans des conditions de faible aération |
| BR112015013188A2 (pt) | 2012-12-07 | 2017-07-11 | Global Bioenergies | método de fermentação otimizado |
| KR102266181B1 (ko) | 2013-09-03 | 2021-06-17 | 피티티 글로벌 케미컬 퍼블릭 컴퍼니 리미티드 | 1,3-프로판디올로부터 아크릴산, 아크릴로니트릴 및 1,4-부탄디올의 제조방법 |
| EP3194603A1 (fr) | 2014-09-17 | 2017-07-26 | Global Bioenergies | Procédé pour la production d'isobutène à partir de 3-méthylcrotonyl-coa |
-
2017
- 2017-12-04 EP EP17807887.9A patent/EP3551679B1/fr active Active
- 2017-12-04 WO PCT/EP2017/081414 patent/WO2018108608A1/fr unknown
- 2017-12-04 CN CN201780085987.3A patent/CN110267997B/zh active Active
- 2017-12-04 US US16/468,414 patent/US20200009041A1/en not_active Abandoned
- 2017-12-04 JP JP2019530752A patent/JP7089516B2/ja active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009149536A (ja) | 2007-12-19 | 2009-07-09 | Toagosei Co Ltd | ２−アクリルアミド−２−メチルプロパンスルホン酸の連続製造方法 |
| JP2012521448A (ja) | 2009-03-25 | 2012-09-13 | クラリアント・ファイナンス・（ビーブイアイ）・リミテッド | アクリル−、メタクリル−もしくはエタクリルアミドアルキルスルホン酸、またはその塩、およびカルボキシアルキルアクリラート、−メタクリラートまたは−エタクリラート、あるいはこれらカルボキシ化合物のオリゴマーに基づくポリマー |
| JP2014511423A (ja) | 2011-03-08 | 2014-05-15 | クラリアント・ファイナンス・（ビーブイアイ）・リミテッド | スルホン酸、アミド及び特定の架橋剤をベースとするポリマー |
Also Published As
| Publication number | Publication date |
|---|---|
| CN110267997A (zh) | 2019-09-20 |
| BR112019011754A2 (pt) | 2019-10-29 |
| CN110267997B (zh) | 2022-07-22 |
| WO2018108608A1 (fr) | 2018-06-21 |
| JP2020513461A (ja) | 2020-05-14 |
| EP3551679B1 (fr) | 2023-05-24 |
| US20200009041A1 (en) | 2020-01-09 |
| EP3551679A1 (fr) | 2019-10-16 |
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